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相关概念视频

GPCRs Regulate Adenylyl Cylase Activity01:09

GPCRs Regulate Adenylyl Cylase Activity

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Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
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Activation and Inactivation of G Proteins01:22

Activation and Inactivation of G Proteins

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Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high...
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GPCR Desensitization01:12

GPCR Desensitization

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G protein-coupled receptor (GPCR) signaling plays a crucial role in cell functioning. GPCR desensitization is an equally essential process. It allows cells to respond to changing environments and regain sensitivity to new stimuli while preventing unnecessary stimulation when no longer needed. Prolonged exposure to stimuli leads to GPCR desensitization. It involves blocking the receptors from binding and activating additional G proteins. This inhibits activation of downstream effectors, thereby...
5.9K
Transducer Mechanism: G Protein–Coupled Receptors01:30

Transducer Mechanism: G Protein–Coupled Receptors

1.9K
G Protein–Coupled Receptors (GPCRs) are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to various stimuli. GPCRs regulate critical physiological pathways and are excellent drug targets for treating diseases such as diabetes, cancer, obesity, depression, or Alzheimer's. Nearly 35% of approved drugs implement their therapeutic effects by selectively interacting with specific GPCRs.
GPCRs are also called heptahelical,...
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G Protein-coupled Receptors01:15

G Protein-coupled Receptors

11.5K
G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
11.5K
G-protein Coupled Receptors01:21

G-protein Coupled Receptors

117.1K
G-protein coupled receptors are ligand binding receptors that indirectly affect changes in the cell. The actual receptor is a single polypeptide that transverses the cell membrane seven times creating intracellular and extracellular loops. The extracellular loops create a ligand specific pocket which binds to neurotransmitters or hormones. The intracellular loops holds onto the G-protein.
117.1K

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相关实验视频

Updated: Jun 13, 2025

A Kinetic Fluorescence-based Ca2+ Mobilization Assay to Identify G Protein-coupled Receptor Agonists, Antagonists, and Allosteric Modulators
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一个GPCR三元复合物的正异构调制.

Wessel A C Burger1,2, Christopher J Draper-Joyce1, Celine Valant1

  • 1Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria 3052, Australia.

Science advances
|September 11, 2024
PubMed
概括

积极的全调节剂稳定了G蛋白合受体 (GPCR) 三元复合体,增强了信号速率. 这一发现促进了对全调节器功能的理解,并有助于治疗设计.

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Measuring G-protein-coupled Receptor Signaling via Radio-labeled GTP Binding
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Methods for the Discovery of Novel Compounds Modulating a Gamma-Aminobutyric Acid Receptor Type A Neurotransmission
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Measuring G-protein-coupled Receptor Signaling via Radio-labeled GTP Binding
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科学领域:

  • 生物化学 生物化学
  • 分子药理学分子药理学
  • 结构生物学 结构生物学

背景情况:

  • 激活后,G蛋白结合受体 (GPCR) 与激动剂和G蛋白形成高亲和三元复合体.
  • 阿洛斯特基调节剂结合了不同的位点,影响了奥托斯特基连接体的亲和力和有效性.
  • 在传统测试中,对活性GPCR-G蛋白质复合体的全调节效应的特征是具有挑战性的.

研究的目的:

  • 为了研究正调节剂对高亲和度GPCR-G蛋白三元复合物的影响.
  • 阐明全调节剂影响正连接体信号传递的机制.
  • 为开发全性疗法提供见解.

主要方法:

  • 净化M2肌肉酸乙胆受体.
  • 将净化的受体复合成纳米磁盘.
  • 生物化学测试以表征三元复合体的形成和信号.

主要成果:

  • 积极的全调节剂稳定了与激动剂结合的高亲和度GPCR-G蛋白三元复合体.
  • 在核酸的存在下,三元复合体的稳定增强了最初的信号速率.
  • 展示了一种在纯化系统中研究这些相互作用的方法.

结论:

  • 基调节剂在稳定活性GPCR-G蛋白质复合体方面发挥着至关重要的作用.
  • 了解这种稳定是理解全联体-受体-G蛋白相互作用的关键.
  • 这些发现有助于合理设计针对GPCRs的新型全oster药物.